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Clinical Research Coordinator Trauma Department (Research Institute)
Clinical Research Coordinator Trauma Department (Research Institute)Research Institute of the MUHC • Montreal, Quebec, Canada
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Clinical Research Coordinator Trauma Department (Research Institute)

Clinical Research Coordinator Trauma Department (Research Institute)

Research Institute of the MUHC • Montreal, Quebec, Canada
Il y a plus de 30 jours
Type de contrat
  • Temps plein
Description de poste

Job Description

RESEARCH INSTITUTE OF THE MUHC

The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal Quebec the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).

Position summary

Under the general supervision of Dr. Kosar Khwaja at the McGill University Health Centre the incumbent is responsible for the general coordination of clinical research projects in the Trauma Department at the Montreal General Hospital.

General Duties

Coordinate local and multi-centered research studies

Assist in the submission of documents to Ethics Boards Pharmacy Contract office and other relevant offices

Maintenance of all documentation of future ongoing and closed projects

Screening consenting and enrolling of patients into clinical studies

Data collection and entering data

Assist in the preparation of manuscripts presentations letters and other scientific reports

Prepare progress reports and statements for granting agencies

Organize investigators meetings and conference calls

Organize regular critical care clinical research meetings for the critical care group at the MUHC

Perform general clerical duties to include but not limited to : photocopying faxing mailing and filing.

Website of the organization

/ Experience

Education : Bachelors Degree

Field of Study : Preferably a Health Science background.

Work Experience : Two (2) years of related experience.

Professional Membership : Yes No

Required Skills

GCP certification and experience with clinical research an asset

Have good skills in written and spoken English and French

Have general knowledge of how hospitals function particularly intensive care units an asset

Knowledge of the Nagano platform for the submission of studies to the RI-MUHC ethics board an asset

Knowledge of the MSSS province-wide multi-centered study submission process an asset

Be capable of working independently with particular attention to detail

Good communication and organizational and interpersonal skills

Able to work with Microsoft Office suite (ACCESS WORD EXCEL and POWERPOINT)

Autonomous flexible sense of ethics and good judgment

Ability to work under minimal supervision

Clinical research experience is an asset.

Required Experience :

IC

Key Skills

CSS,Cloud Computing,Health Education,Actuary,Building Electrician

Employment Type : Unclear

Experience : years

Vacancy : 1

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Research Coordinator • Montreal, Quebec, Canada

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